US6153118A - Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants - Google Patents
Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants Download PDFInfo
- Publication number
- US6153118A US6153118A US09/187,320 US18732098A US6153118A US 6153118 A US6153118 A US 6153118A US 18732098 A US18732098 A US 18732098A US 6153118 A US6153118 A US 6153118A
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- carbon atoms
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- chain alkyl
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
- C09K5/045—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/36—Esters of polycarboxylic acids
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- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/38—Esters of polyhydroxy compounds
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- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/42—Complex esters, i.e. compounds containing at least three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compound: monohydroxy compounds, polyhydroxy compounds, monocarboxylic acids, polycarboxylic acids and hydroxy carboxylic acids
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
- C10M111/04—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
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- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/008—Lubricant compositions compatible with refrigerants
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/24—Only one single fluoro component present
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
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- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/042—Epoxides
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- C10M2207/046—Hydroxy ethers
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Definitions
- This invention relates to a lubricating oil for compressors of refrigerators using therein a hydrogen-containing halogenocarbon as a refrigerant (the oil being hereinafter referred to as "a refrigerator oil for use with a hydrogen-containing halogenocarbon refrigerant") and, more specifically, it relates to such a refrigerator oil which comprises a specific ester as a base oil and is superior in various properties.
- naphthenic mineral oils paraffinic mineral oils, alkylbenzenes, polyglycolic oils, ester oils and mixtures thereof, which have each a kinematic viscosity of 10-200 cSt at 40° C., as well as these oils incorporated with suitable additives have been used as refrigerator oils.
- chlorofluorocarbons (CFCS) type refrigerants such as CFC-11, CFC-12, CFC-113 and HCFC-22, have been used for refrigerators.
- CFCS such as CFC-11, CFC-12 and CFC-113, which are obtained by substituting all the hydrogen atoms of hydrocarbons thereof by halogen atoms including chlorine atoms, may lead to the destruction of the ozone layer, and therefore, the use of the CFCS has been controlled. Accordingly, hydrogen-containing halogenocarbons, such as HFC-134a and HFC-152a, have been being used as substitutes for CFCs. HFC-134a is especially promising as a substitute refrigerant since it is similar in thermodynamic properties to CFC-12 which has heretofore been used in many kinds of refrigerators of home cold-storage chests, air-conditioners and the like.
- Refrigerator oils require various properties, among which their compatibility with refrigerants is extremely important in regard to lubricity and system efficiency in refrigerators.
- conventional refrigerator oils comprising, as the base oils, naphthenic oils, paraffinic oils, alkylbenzenes, heretofore known ester oils and the like, are hardly compatible with hydrogen-containing halogenocarbons such as HFC-134a.
- polyglycolic oils are also known as refrigerator oils for their high viscosity index and are disclosed in, for example, JP-A-57-42119 and JP-A-61-52880 and JP-A-57-51795.
- the polyglycolic oils disclosed in these prior art publications are not fully compatible with HFC-134a thereby raising the same problems as above and rendering them unusable.
- U.S. Pat. No. 4,755,316 discloses polyglycolic refrigerator oils which are compatible with HFC-134a
- U.S. Pat. No. 4,851,144 discloses refrigerator oils comprising a mixture of an ester and a polyglycol which are compatible with HFC-134a.
- the present inventors developed polyglycolic refrigerator oils which have excellent compatibility with HFC-134a as compared with conventional known refrigerator oils, filed an application for a patent for the thus developed polyglycolic refrigerator oils and have already obtained a patent (U.S. Pat. No. 4,948,525) therefor. It has been found, however, that the polyglycolic oils raise problems as to their high compatibility with water and inferior electrical insulating property.
- refrigerator oils used in compressors of home refrigerators and the like are required to have a high electrical insulating property.
- alkylbenzenes and the mineral oils have the highest insulating property, but they are hardly compatible with hydrogen-containing halogenocarbons such as HFC-134a as mentioned above.
- WO 90/12849 describes a composition comprising a hydrogen-containing halogenocarbon and a specific ester lubricant. No refrigerator oil having both high compatibility with hydrogen-containing halogenocarbons such as HFC-134a and a high insulating property has been developed prior to the present invention.
- esters having specific structures have excellent compatibility with hydrogen-containing halogenocarbons such as HFC-134a, and a high electrical insulating property as well as excellent lubricity. This invention is based on this finding.
- the object of this invention is to provide refrigerator oils for use with hydrogen-containing halogenocarbons refrigerants, the oils comprising as a major component (or a base oil) at least one kind of ester having a specific structure and an epoxy compound and having excellent compatibility with hydrogen-containing halogenocarbons such as HFC-134a, high electrical insulating property, high wear resistance, low hygroscopicity, and high thermal and chemical stability.
- the oils comprising as a major component (or a base oil) at least one kind of ester having a specific structure and an epoxy compound and having excellent compatibility with hydrogen-containing halogenocarbons such as HFC-134a, high electrical insulating property, high wear resistance, low hygroscopicity, and high thermal and chemical stability.
- the present invention provides a refrigerator oil for use in compressors using therein a hydrogen-containing halogenocarbon as a refrigerant, consisting essentially of as a base oil at least two esters selected from the group consisting of:
- R 1 -R 4 may be identical with or different from each other and are each a member selected from the group consisting of straight-chain alkyl groups having 3 to 11 carbon atoms, branched-chain alkyl groups having 3 to 15 carbon atoms and cycloalkyl groups having 6 to 12 carbon atoms, the straight-chain alkyl groups being present in a ratio of not more than 60% of the total alkyl groups, and a is an integer of 1 to 3;
- R 5 -R 7 may be identical with or different from each other and are each a member selected from the group consisting of straight-chain alkyl groups having 3 to 11 carbon atoms, branched-chain alkyl groups having 3 to 15 carbon atoms and cycloalkyl groups having 6 to 12 carbon atoms, the straight-chain alkyl groups being present in a ratio of not more than 60% of the total alkyl groups, R 8 is a member selected from the group consisting of methyl, ethyl and propyl groups, and b is an integer of 1 to 3;
- R 1 -R 4 may be identical with, or different from, each other and are each a member selected from the group consisting of straight-chain alkyl groups having 3-11 carbon atoms, preferably 3-7 carbon atoms, branched-chain alkyl groups having 3-15 carbon atoms, preferably 4-11 carbon atoms and cycloalkyl groups having 6-12 carbon atoms, preferably 6-8 carbon atoms.
- the cycloalkyl groups in this invention may include alkylcycloalkyl groups.
- the ratio of the straight-chain alkyl groups to the total alkyl groups is not more than 60%, preferably not more than 50%.
- a is an integer of 1-3.
- the formula (1) illustrates monopentaerythritol esters, dipentaerythritol esters and tripentaerythritol esters.
- R 1 -R 4 are each exemplified by n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, iso-propyl group, iso-butyl group, iso-pentyl group, iso-hexyl group, iso-heptyl group, iso-octyl group, iso-nonyl group, iso-decyl group, iso-undecyl group, iso-dodecyl group, iso-tridecyl group, iso-tetradecyl group, iso-pentadecyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, cyclononyl
- the pentaerythritol esters [I] are esters of pentaerythritol, dipentaerythritol or tripentaerythritol and a monocarboxylic acid, and are ordinarily obtained by the reaction of pentaerythritol, ⁇ dipentaerythritol, tripentaerythritol or a mixture thereof with a mixture of at least one carboxylic acid having the aforementioned alkyl group.
- R 5 -R 7 may be identical with, or different from, each other and are each a group selected from the group consisting of straight-chain alkyl groups having 3-11 carbon atoms, preferably 3-7 carbon atoms, branched-chain alkyl groups having 3-15 carbon atoms, preferably 4-11 carbon atoms and cycloalkyl groups having 6-12 carbon atoms, preferably 6-8 carbon atoms.
- the cycloalkyl groups in this invention may include alkylcycloalkyl groups.
- the ratio of the straight-chain alkyl groups to the total alkyl groups is not more than 60%, preferably not more than 50%.
- R 8 is a member selected from the group consisting of methyl group, ethyl group and propyl group.
- b is an integer of 1-3.
- R 5 -R 7 are each exemplified by n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, iso-propyl group, iso-butyl group, iso-pentyl group, iso-hexyl group, iso-heptyl group, iso-octyl group, iso-nonyl group, iso-decyl group, iso-undecyl group, iso-dodecyl group, iso-tridecyl group, iso-tetradecyl group, iso-pentadecyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, cyclononyl
- the polyol esters [II] are esters of trimethylolethane, trimethylolpropane, trimethylolbutane or a dimer or trimer thereof and a monocarboxylic acid, and are ordinarily obtained by the reaction of trimethylolethane, trimethylolpropane, trimethylolbutane, a dimer or trimer thereof or a mixture thereof with a mixture of at least one carboxylic acid having the aforementioned alkyl group.
- X 1 is a group represented by the general formula --OR 11 or ##STR7## and X 2 is a group represented by the general formula ##STR8## or ##STR9##
- R 9 and R 15 are each a divalent hydrocarbon group having 1-8 carbon atoms, preferably 1-6 carbon atoms
- R 10 and R 12 are each a divalent saturated hydrocarbon group having 2-16 carbon atoms, preferably 2-9 carbon atoms
- R 11 and R 16 are each an alkyl group having 1-15 carbon atoms, preferably 1-12 carbon atoms
- R 13 and R 14 are each an alkyl group having 1-14 carbon atoms, preferably 1-11 carbon atoms.
- c and e are each an integer of 0 or 1 and d is an integer of 0-30, preferably 1-30.
- R 9 and R 15 are each exemplified by a methylene group, ethylene group, propylene group, trimethylene group, butylene group, tetramethylene group, pentamethylene group, hexamethylene group, heptamethylene group, octamethylene group, phenylene group, other unsaturated hydrocarbon groups or the like.
- R 10 and R 12 are each illustrated by nonamethylene group, decamethylene group, undecamethylene group, dodecamethylene group, tridecamethylene group, tetradecamethylene group, pentadecamethylene group, hexadecamethylene group, cyclohexylene group or the like in addition to the above alkylene groups (except for methylene group).
- R 13 and R 14 are each concretely exemplified by straight- or branched-chain alkyl groups, such as methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group or tetradecyl group.
- R 11 and R 16 are each illustrated by a straight- or branched-chain alkyl group, such as a pentadecyl group, in addition to any one of the above alkyl groups.
- the method for producing the esters [III] is not particularly limited.
- a mixture of the esters [III] can be produced by the esterification reaction of (i) a diol having none of ether linkages in the branched-chains thereof with (ii) a dicarboxylic acid and (iii) a monocarboxylic acid and/or (iv) a monohydric alcohol.
- the esters [III] are also produced by the reaction of the diol (i) with the monocarboxylic acid (iii) or the reaction of the dicarboxylic acid (ii) with the monohydric alcohol (iii).
- the diols (i) used herein are those having 2-16 carbon atoms and are exemplified by alkylene glycols such as ethylene glycol, propylene glycol, butylene glycol, trimethylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, heptamethylene glycol, octamethylene glycol, nonamethylene glycol, decamethylene glycol, neopentyl glycol, 2-ethyl-2-methyl-1,3-propanediol, 2-methyl-2-propyl-1,3-propanediol, 2,2-dimethyl-1,3-propanediol, 2-butyl-2-ethyl-1,3-propanediol, 3-methyl-1,5-pentanediol, 2,4-pentanediol, 2-methyl-2,4-pentanediol, 2-methyl-1,6-hexane, 1,4
- the dicarboxylic acids (ii) used herein are those having 2-10 carbon atoms and are exemplified by saturated aliphatic dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, methylmalonic acid, ethylmalonic acid, dimethylmalonic acid, methylsuccinic acid, 2,2-dimethylsuccinic acid, 2,3-dimethylsuccinic acid, 2-ethyl-2-methylsuccinic acid, 2-methylglutaric acid, 3-methylglutaric acid, 3,3-dimethylglutaric acid and 3-methyladipic acid; unsaturated aliphatic dicarboxylic acids such as maleic acid, fumaric acid, itaconic acid, citraconic acid and mesaconic acid; and aromatic dicarboxylic acids such as phthalic acid, isophthalic acid and
- the monocarboxylic acids (iii) used herein are those having 2-15 carbon atoms and are exemplified by acetic acid, propionic acid, butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, 3-methylbutanoic acid, 2-methylbutanoic acid, 2-ethylhexanoic acid, 2,4-dimethylpentanoic acid, 3,3,5-trimethylhexanoic acid and benzoic acid.
- the monohydric alcohols (iv) used herein are those having 1-15 carbon atoms and are exemplified by methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, octanol, nonanol, decanol, unedecanol, dodecanol, tridecanol, tetradecanol, pentadecanol, isopropanol, isobutanol, 2-methyl-1-butanol, 2,2-dimethyl-1-propanol, 3,3-dimethyl-1-butanol, 2-methyl-1-pentanol, 3-methyl-1-pentanol, 2,4,4-trimethyl-1-pentanol, 2,2,4-trimethyl-1-pentanol, 2-ethyl-4-methyl-1-pentanol and 2-ethyl-1-hexanol.
- the molecular weight of the ester [III] is not particularly limited, but the number average molecular weight of the ester [III] is in the range of preferably 200-3000, more preferably 300-2000, to improve the compressor in sealability
- neopentyl type polyhydric alcohols (a) having 5-6 carbon atoms and 3-4 hydroxyl groups are illustrated by trimethylolethane, trimethylolpropane and pentaerythritol.
- the monocarboxylic acids (b) preferably used herein are those having 2-15 carbon atoms and are exemplified by acetic acid, propionic acid, butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid and pentadecanoic acid.
- carboxylic acids may be either straight-chain or branched-chain ones, but it is preferable to use the latter having a branched-chain structure in an amount of not less than 50 mol %, preferably not less than 60 mol %.
- the dicarboxylic acids (c) used herein are those having 2-10 carbon atoms and are exemplified by saturated aliphatic dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, methylmalonic acid, ethylmalonic acid, dimethylmalonic acid, methylsuccinic acid, 2,2-dimethylsuccinic acid, 2,3-dimethylsuccinic acid, 2-ethyl-2-methylsuccinic acid, 2-methylglutaric acid, 3-methylglutaric acid and 3-methyladipic acid; unsaturated aliphatic dicarboxylic acids such as maleic acid, fumaric acid, itaconic acid, citraconic acid and mesaconic acid; and aromatic dicarboxylic acids such as phthalic acid, terephthalic acid and isophthalic acid.
- esters [IV] are produced by the esterification reaction of the aforesaid component (a) with the component (b) and the component (c) under ordinary esterification conditions, for example, in the presence of an acid catalyst such as sulfuric acid and at a temperature of 100-180° C.
- ester [IV] The chemical structure of the ester [IV] according to the present invention is illustrated by the following general formula (6) ##STR10## wherein X 3 and X 4 may be identical with, or different from, each other and are each an alkyl group having 1-4 carbon atoms or a group represented by the general formula ##STR11## R 26 -R 29 and R 31 may be identical with, or different from each other and are each an alkyl group having 4-15 carbon atoms; R 30 is an alkylene group having 1-8 carbon atoms; j is an integer of 0 or 1; and k is an integer of 1-5.
- the molecular weight of the polyol ester [IV] is not particularly limited, but the number average molecular weight of the ester [IV] is in the range of preferably 200-3000, more preferably 300-2000, to improve the compressor in sealability.
- the products obtained by the methods as mentioned above may be refined to remove the by-products and/or unreacted reactants, but the by-products and/or unreacted reactants may be present in small amounts in the refrigerator oils of the present invention as far as they do not impair the excellent performances thereof.
- esters [I]-[IV] mentioned above are used jointly as a mixture of at least two kinds of the esters.
- the kinematic viscosities of the esters according to the present invention are in the range of preferably 2-150 cSt, more preferably 5-100 cSt at 100° C.
- the refrigerator oil of the present invention may comprise as the only base oil at least one member selected from the above esters [I]-[IV] and, as required, it may additionally comprise other base oils for refrigerator oils.
- other base oils preferable ones are illustrated as follows:
- R 17 and R 18 are each a hydrogen atom or an alkyl group having 1-18 carbon atoms
- R 19 is an alkylene group having 2-4 carbon atoms
- f is an integer of 5-70
- a polyoxyalkylene glycol glycerol ether represented by the general formula (5) ##STR13## wherein R 20 -R 22 are each a hydrogen atom or an alkyl group having 1-18 carbon atoms, R 23 -R 25 are each an alkylene group having 2-4 carbon atoms and g-i are each an integer of 5-7.
- refrigerator oil of this invention may be incorporated with paraffinic mineral oils, naphthenic mineral oils, poly ⁇ -olefins, alkylbenzenes and the like, but, in this case, the resulting mixed oil will be lowered in compatibility with hydrogen-containing halogonocarbons.
- esters [I]-[IV] should be present in the resulting mixed oil in a ratio of usually more than 50% by weight, preferably not less than 70% by weight of the total amount of the mixed oil.
- the epoxy compound used herein is preferably selected from the group consisting of phenylglycidyl ether epoxy compounds, alkylglycidyl ether epoxy compounds, glycidyl ester epoxy compounds, aryloxirane compounds, alkyloxirane compounds, alicyclic epoxy compounds, epoxidized fatty acid monoesters and epoxidized vegetable oils.
- the said phenylglycidyl ether epoxy compounds used herein include phenylglycidyl ether and derivatives thereof such as alkylphenylglycidyl ethers.
- the said alkylphenylglycidyl ethers are those having 1 to 3 alkyl groups having 1 to 13 carbon atoms, among which are preferred those having an alkyl group having 4 to 10 carbon atoms, such as n-butylphenylglycidyl ether, i-butylphenylglycidyl ether, sec-butylphenylglycidyl ether, tert-butylphenylglycidyl ether, pentylphenylglycidyl ether, hexylphenylglycidyl ether, heptylphenylglycidyl ether, octylphenylglycidyl ether, nonylphenylglycidyl
- the alkylglycidyl ether epoxy compounds include decylglycidyl ether, undecylglycidyl ether, dodecylglycidyl ether, tridecylglycidyl ether, tetradecylglycidyl ether, 2-ethylhexylglycidyl ether, neopentyl glycol diglycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol tetraglycidyl ether, 1,6-hexanediol diglycidyl ether, sorbitol polyglycidyl ether, polyalkylene glycol monoglycidyl ethers and polyalkylene glycol diglycidyl ethers.
- the glycidyl ester epoxy compounds include phenylglycidyl esters, alkylglycidyl esters and alkenylglycidyl esters with glycidyl 2,2-dimethyl octanoate, glycidyl benzoate, glycidyl acrylate, glycidyl methacrylate and the like being preferred.
- the aryloxirane compounds include 1,2-epoxystyrene and alkyl-1,2-epoxystyrene.
- the alkyloxirane compounds include 1,2-epoxybutane, 1,2-epoxypentane, 1,2-epoxyhexane, 1,2-epoxyheptane, 1,2-epoxyoctane, 1,2-epoxynonane, 1,2-epoxydecane, 1,2-epoxyundecane, 1,2-epoxydodecane, 1,2-epoxytridecane, 1,2-epoxytetradecane, 1,2-epoxypentadecane, 1,2-epoxyhexadecane, 1,2-epoxyheptadecane, 1,1,2-epoxyoctadecane, 2-epoxynonadecane and 1,2-epoxyeicosane.
- the alicyclic epoxy compounds include 1,2-epoxycyclohexane, 1,2-epoxycyclopentane, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate, bis(3,4-epoxycyclohexylmethyl) adipate, exo-2,3-epoxynorbornane, bis(3,4-epoxy-6-methylcyclohexylmethyl) adipate, 2-(7-oxabicyclo[4.1.0]hept-3-yl)-spiro(1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0]heptane, 4-(1'-methylepoxyethyl)-1,2-epoxy-2-methylcyclohexane and 4-epoxyethyl-1,2-epoxycyclohexane.
- the epoxidized fatty acid monoesters include esters of an epoxidized fatty acid having 12 to 20 carbon atoms and an alcohol having 1 to 8 carbon atoms, phenol or an alkylphenol.
- esters of an epoxidized fatty acid having 12 to 20 carbon atoms and an alcohol having 1 to 8 carbon atoms, phenol or an alkylphenol may preferably be used.
- the epoxidized vegetable oils include epoxidized compounds of vegetable oils such as soybean oil, linseed oil and cottonseed oil.
- the preferable ones include phenylglycidyl ether epoxy compounds, alkylglycidyl ether epoxy compounds, glycidyl ester epoxy compounds and alicyclic epoxy compounds.
- these epoxy compounds be incorporated in the refrigerator oil of the present invention in a ratio of 0.1-5.0% by weight, preferably 0.2-2.0% by weight, of the total amount of the refrigerator oil.
- the refrigerator oil composition according to this invention may be incorporated further with at least one kind of a phosphorus compound selected from the group consisting of phosphoric esters, acid phosphoric esters, amine salts of acid phosphoric esters, chlorinated phosphoric esters and phosphorous esters, to improve the oil composition in wear resistance and load resistance.
- phosphorus compounds are esters of phosphoric acid or phosphorous acid and an alkanol or a polyether type alcohol, or derivatives of the esters.
- the phosphoric esters are exemplified by tributyl phosphate, triphenyl phosphate and tricresyl phosphate.
- the acid phosphoric esters are exemplified by ditetradecyl acid phosphate, dipentadecyl acid phosphate, dihexadecyl acid phosphate, diheptadecyl acid phosphate and dioctadecyl acid phosphate.
- the amine salts of acid phosphoric esters are exemplified by salts of the above acid phosphoric esters and amines such as methylamine, ethylamine, propylamine, butylamine, pentylamine, hexylamine, heptylamine, octylamine, dimethylamine, diethylamine, dipropylamine, dibutylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, trimethylamine, triethylamine, tripropylamine, tributylamine, tripentylamine, trihexylamine, triheptylamine and trioctylamine.
- amines such as methylamine, ethylamine, propylamine, butylamine, pentylamine, hexylamine, heptylamine, octylamine, dimethylamine, diethylamine, diprop
- the chlorinated phosphoric esters are exemplified by tris-dichloropropyl phosphate, tris.chloroethyl phosphate, polyoxyalkylene.bis[di(chloroalkyl)] phosphate and tris.chlorophenyl phosphate.
- the phosphorous esters are exemplified by dibutyl phosphite, tributyl phosphite, dipentyl phosphite, tripentyl phosphite, dihexyl phosphite, trihexyl phosphite, diheptyl phosphite, triheptyl phosphite, dioctyl phosphite, trioctyl phosphite, dinonyl phosphite, didecyl phosphite, diundecyl phosphite, triundecyl phosphite, didodecyl phosphite, tridodecyl phosphite, diphenyl phosphite, triphenyl phosphite, dicresyl phosphite, tricresyl phosphite
- the refrigerator oil may be incorporated, as required, with heretofore known additives for a refrigerator oil, which include phenol-type antioxidants such as di-tert.-butyl-p-cresol and bisphenol A; amine-type antioxidants such as phenyl- ⁇ -naphthylamine and N,N-di(2-naphthyl)-p-phenylenediamine; wear resistant additives such as zinc dithiophosphate; extreme pressure agents such as chlorinated paraffin and sulfur compounds; oiliness improvers such as fatty acids; antifoaming agents such as silicone-type ones; and metal inactivators such as benzotriazole.
- phenol-type antioxidants such as di-tert.-butyl-p-cresol and bisphenol A
- amine-type antioxidants such as phenyl- ⁇ -naphthylamine and N,N-di(2-naphthyl)-p-phenylenediamine
- wear resistant additives such
- the refrigerator oils of this invention comprising at least one of the esters [I]-[IV] as the base oil should have such viscosity and pour point as those which are normally suitable for an ordinary refrigerator oil, but they should have a pour point of not higher than -10° C., preferably -20° C. to -80° C., to prevent them from solidification at a low temperature.
- they should desirably have a kinematic viscosity of not less than 2 cSt, preferably not less than 3 cSt at 100° C., to keep the sealability of the compressor when used, while they should desirably have a kinematic viscosity of not more than 150 cSt, preferably not more than 100 cSt at 100° C., in veiw of their fluidity at a low temperature and the efficiency of heat exchange in the evaporator when used.
- the refrigerants which may be used in refrigerators in which the lubricating oils (refrigerator oils) of the present invention are suitably used include hydrogen-containing halogenocarbons such as alkane fluorides having 1-3 carbon atoms, preferably 1-2 carbon atoms and/or alkane chloride fluoride having 1-3 carbon atoms, preferably 1-2 carbon atoms.
- HFCs chlorine-free type halogenocarbons
- HFC-32 difluoromethane
- HFC-23 trifluoromethane
- pentafluoroethane HFC-125
- 1,1,2,2-tetrafluoroethane HFC-134
- 1,1,1,2-tetrafluoroethane HFC-134a
- 1,1,1-trifluoroethane HFC-143a
- 1,1-difluoroethane HFC-152a
- HCFCs chlorine-containing type halogenocarbons
- monochlorodifluoromethane HCFC-22
- 1-chloro-1,1-difluoroethane HCFC-142b
- dichlorotrifluoroethane HCFC-123
- monochlorotetrafluoroethane HCFC-124
- the chlorine-free type halogenocarbons such as HFC-32, HFC-23, HFC-125, HFC-134, HFC-134a and HFC-152a, are preferable in view of the environmental problems.
- the refrigerant used may suitably be selected from these halogenocarbons mentioned above depending on the purpose for which the resulting refrigerant is used as well as the properties which are desirable for the resulting refrigerant.
- the preferable refrigerants are exemplified by HFC-134a; a mixture of HFC-134a (60-80 wt %) and HFC-32 (40-20 wt %); a mixture of HFC-32 (50-70 wt %) and HFC-125 (50-30 wt %); a mixture of HFC-134a (60 wt %), HFC-32 (30 wt %) and HFC-125 (10 wt %); a mixture of HFC-134a (52 wt %), HFC-32 (23 wt %) and HFC-125 (25 wt %); and a mixture of HFC-143a (52 wt %), HFC-125 (44 wt %) and HFC-134a (4 wt %).
- the refrigerator oil of the present invention When used in a refrigerator, it is usually present in the form of a fluid composition for the refrigerator, which is a mixture of the refrigerator oil and a chlorine-free type halogenocarbon such as an alkane fluoride and/or an alkane chloride fluoride as mentioned above.
- a fluid composition for the refrigerator which is a mixture of the refrigerator oil and a chlorine-free type halogenocarbon such as an alkane fluoride and/or an alkane chloride fluoride as mentioned above.
- the present invention relates to a fluid composition for a refrigerator, which comprises a chlorine-free type halogenocarbon refrigerant and a refrigerator oil according to the present invention.
- the mixing ratio of the refrigerator oil and the refrigerant in the resulting composition is not particularly limited, but the refrigerator oil is usually comprised in an amount of 1-500 parts by weight, preferably in an amount of 2-400 parts by weight, based on 100 parts by weight of the refrigerant.
- the refrigerator oils of the present invention are excellent in compatibility with the hydrogen-containing halogenocarbons as compared with the heretofore known refrigerator oils. Further, the refrigerator oils of the present invention are excellent which have not only high compatibility with the hydrogen-containing halogenocarbons and high electrical insulating property but also high lubricity, low hygroscopicity and high thermal and chemical stability.
- the refrigerator oils of the present invention may particularly preferably be used in refrigerators, air-conditioners, dehumidifiers, cold-storage chests, freezers, freeze and refrigeration warehouses, automatic vending machines, showcases, cooling units in chemical plants, and the like which have a reciprocating or rotary compressor. Further, the above refrigerator oils may also preferably be used in refrigerators having a centrifugal compressor.
- Base oils 1-6 base oils according to this invention
- Base oils 7-22 comparative base oils
- Base oil 1 A mixture of 50 parts by weight of a tetraester of pentaerythritol (1 mol), 2-ethylhexanoic acid (2 mol) and 3,5,5-trimethylhexanoic acid (2 mol), and 50 parts by weight of a triester of trimethylolpropane (1 mol), 2-ethylhexanoic acid (1.5 mol) and 3,5,5-trimethylhexanoic acid (1.5 mol):
- Base oil 3 A mixture of 50 parts by weight of a tetraester of pentaerythritol (1 mol), 2-ethylhexanoic acid (2 mol) and 3,5,5-trimethylhexanoic acid (2 mol), and 50 parts by weight of an ester having an average molecular weight of 880 and a kinematic viscosity at 100° C. of 12.7 cSt, obtained by the reaction of 2 moles of pentaerythritol with 1 mole of succinic acid, 1 mole of glutaric acid, 3 moles of iso-pentanoic acid and 3 moles of iso-hexanoic acid
- Base oil 6 A mixture of 50 parts by weight of a diester of 3-methyl-1,5-pentanediol and 3,5,5-trimethylhexanoic acid, and 50 parts by weight of an ester having an average molecular weight of 880 and a kinematic viscosity at 100° C. of 12.7 cSt, obtained by the reaction of 2 moles of pentaerythritol with 1 mole of succinic acid, 1 mole of glutaric acid, 3 moles of iso-pentanoic acid and 3 moles of iso-hexanoic acid
- Base oil 17 A mixture of 95 parts by weight of the same ester as in Base oil 1 and 5 parts by weight of the same ester as in Base oil 10
- Base oil 18 A mixture of 95 parts by weight of the same ester as in Base oil 2 and 5 parts by weight of the same ester as in Base oil 10
- Base oil 19 A mixture of 95 parts by weight of the same ester as in Base oil 3 and 5 parts by weight of the same ester as in Base oil 10
- Base oil 20 A mixture of 95 parts by weight of the same ester as in Base oil 4 and 5 parts by weight of the same ester as in Base oil 10
- Base oil 21 A mixture of 95 parts by weight of the same ester as in Base oil 5 and 5 parts by weight of the same ester as in Base oil 10
- Base oil 22 A mixture of 95 parts by weight of the same ester as in Base oil 6 and 5 parts by weight of the same ester as in Base oil 10
- the refrigerator oils of Examples 1-6 according to the present invention each of which has a composition indicated in the following Table 1 were prepared and then evaluated for their performances that are their miscibility with HFC-134a, insulating property, wear resistance, hygroscopicity and thermal and chemical stability by the following respective test methods. The results thus obtained are indicated in Table 1.
- test oils were each measured for specific volume resistivity at 25° C. in accordance with JIS C 2101.
- test oils were each applied to a test journal for measuring the amount of the test journal worn by having the journal run in at a test oil temperature of 100° C. under a load of 150 lb for 1 minute and then running it under a load of 250 lb for 2 hours in accordance with ASTM D 2670.
- test oils Thirty grams (30 g) of each of the test oils were placed in a 300-ml beaker, allowed to stand for 7 days in an air-conditioned bath maintained at a temperature of 60° C. and a humidity of 30% and then measured for water content by the Karl-Fischer method.
- test oils Fifty grams (50 g) of each of the test oils (Examples 1-6 and Comparative Examples 11-16) indicated in Table 1 were placed in a 100-ml beaker, and then allowed to stand for 168 hours in an air-conditioned bath maintained at a temperature of 25° C. and a relative humidity of 80%. Next, an equi-volume mixture of each of these test oils and the refrigerant (HFC-134a) was sealed, together with copper, iron and aluminum catalysts, in a glass tube and then heated to 175° C. for 168 hours to observe whether the state of the test oil has been changed or not.
- HFC-134a refrigerant
- Table 1 further shows that the ethers of Comparative Examples 3 and 4 as well as the polyoxypropylene glycols of Comparative Examples 5 and 6 are excellent in miscibility with the refrigerant, but these ethers and glycols are inferior in insulating property thereby rendering them unusable for hermetic type compressors. Still further, Table 1 shows that the ethers and glycols of Comparative Examples 3-6 have hygroscopicity 5-10 times that of the refrigerator oils of Examples 1-6 and are also inferior in electrical insulating property, ice choke, wear resistance, stability and the like to the refrigerator oils of the Examples.
- the FALEX wear test shows that the refrigerator oils of Examples 1-6 are at least equal in wear resistance to those of Comparative Examples 3-6.
- the refrigerator oils of Comparative Examples 11-16 each of which contains at least a polypropylene glycol monoalkyl ether and an epoxy compound have a disadvantage that a precipitate which is insoluble into the base oil and the refrigerant is formed in the refrigerator oils due to deterioration of the epoxy compound during the storage under a high humidity.
- the formed precipitate makes the refrigerator oil white-turbid and leads to danger of blocking an expansion valve and/or a capillary tube in a refrigerator system in which the above refrigerator oils of Comparative Examples 11-16 is used.
- the refrigerator oils of Comparative Examples 11-16 have lower resistivity and higher hygroscopicity than any one of refrigerator oils of the present invention.
- the refrigerator oils (Examples 1-6) of the present invention are free from the generation of such a precipitate even if they are stored under a high humidity. Therefore, in a case where the refrigerator oil of the present invention is used in a refrigerator system, there is no danger as mentioned above.
- the refrigerator oils of Comparative Examples 17-22 which are free from epoxy compounds are equivalent to those of Examples 1-6 of the present invention in miscibility with HFC-134a, insulating property, wear resistance and hygroscopicity, but, as is apparent from the results of the sealed tube test, the refrigerator oils of Comparative Examples 17-22 are quite inferior in thermal and chemical stability as compared with the refrigerator oils of the present invention.
- the refrigerator oils of the present invention are suitable for use in refrigerators using therein a hydrogen-containing halogenocarbon as a refrigerant and are excellent in electrical insulating property, wear resistance, nonhygroscopicity and thermal and chemical stability.
- the refrigerator oils of the present invention excellently have all properties which are important for refrigerator oils.
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Abstract
Description
C.brket open-st.CH.sub.2 --OOC--R.sub.1 ].sub.4 ##STR14## or ##STR15## and
C.sub.2 H.sub.5 --C.brket open-st.CH.sub.2 --OOC--R.sub.1 ].sub.3 ##STR16## [Base oil 2] A mixture of 50 parts by weight of a tetraester of pentaerythritol (1 mol), 2-ethylhexanoic acid (2 mol) and 3,5,5-trimethylhexanoic acid (2 mol), and 50 parts by weight of a diester of 3-methyl-1,5-pentanediol and 3,5,5-trimethylhexanoic acid:
C.brket open-st.CH.sub.2 --OOC--R.sub.1 ].sub.4
TABLE 1
__________________________________________________________________________
Miscible
Examples Kinematic
Temp. Rang
Resisti-
Falex test
Hygro-
. Epoxy compounds*
viscosity
with vity Amount of
scopicity
Comparative
Base Amount
@ 100° C.
HFC-134a
@ 25° C.
journal
30° C., 60%
Examples
oils
Kind (In wt %)
(mm.sup.2 /s)
(° C.)
(Ωcm)
worn (mg)
(%)
__________________________________________________________________________
Example 1
1 PGE 1.0 6.5 -32˜CT**
3.8 × 10.sup.14
25 0.21
Example 2
2 s-BuPGE 1.0 4.5 -30˜CT**
4.0 × 10.sup.14
25 0.21
Example 3
3 t-BuPGE 1.0 9.4 -30˜CT**
2.4 × 10.sup.14
24 0.17
Example 4
4 DODECYLGEs
1.0 5.0 -34˜CT**
3.9 × 10.sup.14
24 0.21
Example 5
5 DECYLGEs
1.0 9.8 -32˜CT**
2.3 × 10.sup.14
22 0.18
Example 6
6 EPCH 1.0 7.8 -30˜CT**
2.3 × 10.sup.14
19 0.18
Comp. Ex. 1
7 none -- 5.1 Immiscible
3.8 × 10.sup.15
23 0.01
Comp. Ex. 2
8 none -- 4.8 Immiscible
6.4 × 10.sup.15
25 0.01
Comp. Ex. 3
9 none -- 4.9 <-70˜97
1.1 × 10.sup.11
40 1.31
Comp. Ex. 4
10 none -- 10.8 <-70˜56
1.2 × 10.sup.11
35 1.01
Comp. Ex. 5
11 none -- 10.6 <-70˜64
5.6 × 10.sup.10
38 2.30
Comp. Ex. 6
12 none -- 22.4 -51˜32
4.8 × 10.sup.10
30 1.81
Comp. Ex. 7
13 none -- 6.1 Immiscible
2.1 × 10.sup.14
25 0.21
Comp. Ex. 8
14 none -- 4.9 Immiscible
-- -- --
Comp. Ex. 9
15 none -- 5.4 Immiscible
-- -- --
Comp. Ex. 10
16 none -- 4.4 Immiscible
-- -- --
Comp. Ex. 11
17 PGE 1.0 6.8 -33˜CT**
6.9 × 10.sup.12
28 0.23
Comp. Ex. 12
18 s-BuPGE 1.0 4.8 -30˜CT**
7.3 × 10.sup.12
27 0.23
Comp. Ex. 13
19 t-BuPGE 1.0 9.8 -31˜CT**
5.8 × 10.sup.12
26 0.19
Comp. Ex. 14
20 DODECYLGEs
1.0 5.2 -34˜CT**
6.5 × 10.sup.12
27 0.23
Comp. Ex. 15
21 DECYLGEs
1.0 10.2 -32˜CT**
1.2 × 10.sup.12
25 0.20
Comp. Ex. 16
22 EPCH 1.0 8.0 -30˜CT**
2.8 × 10.sup.12
23 0.20
Comp. Ex. 17
1 none -- 6.6 -32˜CT**
4.1 × 10.sup.14
26 0.20
Comp. Ex. 18
2 none -- 4.6 -30˜CT**
4.0 × 10.sup.14
25 0.20
Comp. Ex. 19
3 none -- 9.5 -30˜CT**
2.8 × 10.sup.14
23 0.16
Comp. Ex. 20
4 none -- 5.0 -34˜CT**
4.1 × 10.sup.14
24 0.20
Comp. Ex. 21
5 none -- 9.9 -32˜CT**
2.6 × 10.sup.14
21 0.17
Comp. Ex. 22
6 none -- 7.7 -30˜CT**
2.4 × 10.sup.14
20 0.18
__________________________________________________________________________
Examples
. Sealed tube test
Comparative
Oil
Catalyst Appearance
Examples
color
Cu Fe Al of test oil
__________________________________________________________________________
Example 1
1 No change
No change
No change
No change
Example 2
1 No change
No change
No change
No change
Example 3
1 No change
No change
No change
No change
Example 4
1 No change
No change
No change
No change
Example 5
1 No change
No change
No change
No change
Example 6
1 No change
No change
No change
No change
Comp. Ex. 1
-- -- -- -- --
Comp. Ex. 2
-- -- -- -- --
Comp. Ex. 3
-- -- -- -- --
Comp. Ex. 4
-- -- -- -- --
Comp. Ex. 5
-- -- -- -- --
Comp. Ex. 6
-- -- -- -- --
Comp. Ex. 7
-- -- -- -- --
Comp. Ex. 8
-- -- -- -- --
Comp. Ex. 9
-- -- -- -- --
Comp. Ex. 10
-- -- -- -- --
Comp. Ex. 11
2 Luster decreased
Luster decreased
No change
Wite-turbid
Comp. Ex. 12
2 Luster decreased
Luster decreased
No change
Wite-turbid
Comp. Ex. 13
2 Luster decreased
No change
No change
Wite-turbid
Comp. Ex. 14
2 Luster decreased
Luster decreased
No change
Wite-turbid
Comp. Ex. 15
2 Luster decreased
No change
No change
Wite-turbid
Comp. Ex. 16
2 Luster decreased
Luster decreased
No change
Wite-turbid
Comp. Ex. 17
1 No change
Luster decreased
No change
--
Comp. Ex. 18
1 No change
Luster decreased
No change
--
Comp. Ex. 19
1 No change
Luster decreased
No change
--
Comp. Ex. 20
1 No change
Luster decreased
No change
--
Comp. Ex. 21
1 No change
Luster decreased
No change
--
Comp. Ex. 22
1 No change
Luster decreased
No change
--
__________________________________________________________________________
*PGE: Phenyl Glycidyl Ether
sBuPGE: sButylphenyl Glycidyl Ether
tBuPGE: tButylphenyl Glycidyl Ether
DODECYLGE: Dodecyl Glycidyl Ether
DECYLGEs: Glycidyl 1,1Dimethyloctanoate
EPCH: 1,2Epxoyclohexane
**CT; Critical temperature of HFC134a (102° C.)
Claims (18)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/187,320 US6153118A (en) | 1989-12-28 | 1998-11-06 | Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants |
Applications Claiming Priority (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1-341245 | 1989-12-28 | ||
| JP1341245A JP2627564B2 (en) | 1989-12-28 | 1989-12-28 | Refrigeration oil for non-chlorinated chlorofluorocarbon refrigerant |
| JP1-341244 | 1989-12-28 | ||
| JP34124489A JP3012907B2 (en) | 1989-12-28 | 1989-12-28 | Refrigeration oil for non-chlorinated chlorofluorocarbon refrigerant |
| JP10577290A JPH044294A (en) | 1990-04-20 | 1990-04-20 | Refrigerator oil for non-chlorine based fluorocarbon refrigeration medium |
| JP2-105772 | 1990-04-20 | ||
| JP2-121133 | 1990-05-14 | ||
| JP12113390A JPH0420597A (en) | 1990-05-14 | 1990-05-14 | Refrigerator oil for hydrofluorocarbon refrigerant |
| US63405490A | 1990-12-26 | 1990-12-26 | |
| US1917793A | 1993-01-28 | 1993-01-28 | |
| US19328194A | 1994-02-08 | 1994-02-08 | |
| US08/539,001 US6582621B1 (en) | 1989-12-28 | 1995-10-04 | Refrigerator oils for use with chlorine-free fluorocarbon refrigerants |
| US09/187,320 US6153118A (en) | 1989-12-28 | 1998-11-06 | Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/539,001 Continuation-In-Part US6582621B1 (en) | 1989-12-28 | 1995-10-04 | Refrigerator oils for use with chlorine-free fluorocarbon refrigerants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US6153118A true US6153118A (en) | 2000-11-28 |
Family
ID=46255248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/187,320 Expired - Fee Related US6153118A (en) | 1989-12-28 | 1998-11-06 | Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US6153118A (en) |
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6258293B1 (en) * | 1990-11-16 | 2001-07-10 | Hitachi, Ltd. | Refrigeration cycle |
| US6551524B2 (en) | 1992-06-03 | 2003-04-22 | Cognis Corporation | Polyol ester lubricants, especially those compatible with mineral oils, for refrigerating compressors operating at high temperatures |
| US6551523B1 (en) | 1995-06-07 | 2003-04-22 | Cognis Corporation | Blended polyol ester lubricants for refrigerant heat transfer fluids |
| US6582621B1 (en) * | 1989-12-28 | 2003-06-24 | Nippon Mitsubishi Oil Corporation | Refrigerator oils for use with chlorine-free fluorocarbon refrigerants |
| US6666985B2 (en) | 1992-06-03 | 2003-12-23 | Cognis Corporation | Polyol ester lubricants for hermetically sealed refrigerating compressors |
| US6692654B2 (en) * | 1998-09-29 | 2004-02-17 | Nippon Mitsubishi Oil Corporation | Refrigerating machine oil |
| US20040092410A1 (en) * | 2002-07-12 | 2004-05-13 | Carr Dale D. | High viscosity synthetic ester lubricant base stock |
| US20050148476A1 (en) * | 2004-01-07 | 2005-07-07 | The Lubrizol Corporation | Automatic transmission fluids with phthalic acid corrosion inhibitor |
| US6998065B1 (en) * | 1989-12-28 | 2006-02-14 | Nippon Mitsubishi Oil Corporation | Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants |
| US7018558B2 (en) | 1999-06-09 | 2006-03-28 | Cognis Corporation | Method of improving performance of refrigerant systems |
| US7052626B1 (en) * | 1989-12-28 | 2006-05-30 | Nippon Mitsubishi Oil Corporation | Fluid compositions containing refrigeration oils and chlorine-free fluorocarbon refrigerants |
| US20100038583A1 (en) * | 2007-02-27 | 2010-02-18 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerator |
| US20100038582A1 (en) * | 2007-02-27 | 2010-02-18 | Yuji Shimomura | Refrigerator oil and working fluid composition for refrigerator |
| US20100051854A1 (en) * | 2007-03-27 | 2010-03-04 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerating machine |
| US20100117022A1 (en) * | 2008-11-13 | 2010-05-13 | Chemtura Corporation | Lubricants for refrigeration systems |
| US20100282999A1 (en) * | 2007-10-29 | 2010-11-11 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerating machine |
| US8858820B2 (en) | 2011-10-07 | 2014-10-14 | American Pacific Corporation | Bromofluorocarbon compositions |
| US20150090921A1 (en) * | 2012-03-23 | 2015-04-02 | Kh Neochem Co., Ltd. | Mixed ester |
| EP2832813A4 (en) * | 2012-03-30 | 2015-11-11 | Idemitsu Kosan Co | REFRIGERANT COMPOSITION AND METHOD FOR DECREASING DECOMPOSITION OF FLUORINATED HYDROCARBON |
| US9410105B2 (en) | 2012-11-16 | 2016-08-09 | Basf Se | Lubricant compositions comprising epoxide compounds |
| US10000722B2 (en) | 2013-09-12 | 2018-06-19 | Idemitsu Kosan Co., Ltd. | Refrigeration machine oil composition |
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| WO1990012849A1 (en) * | 1989-04-25 | 1990-11-01 | The Lubrizol Corporation | Liquid compositions containing carboxylic esters |
| US5185092A (en) * | 1990-01-31 | 1993-02-09 | Tonen Corporation | Lubricating oil for refrigerator |
| US5202044A (en) * | 1990-09-12 | 1993-04-13 | Kao Corporation | Working fluid composition for refrigerating machine |
| US5395544A (en) * | 1992-07-04 | 1995-03-07 | Kao Corporation | Ester-containing working fluid composition for refrigerating machine |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1990012849A1 (en) * | 1989-04-25 | 1990-11-01 | The Lubrizol Corporation | Liquid compositions containing carboxylic esters |
| US5185092A (en) * | 1990-01-31 | 1993-02-09 | Tonen Corporation | Lubricating oil for refrigerator |
| US5202044A (en) * | 1990-09-12 | 1993-04-13 | Kao Corporation | Working fluid composition for refrigerating machine |
| US5395544A (en) * | 1992-07-04 | 1995-03-07 | Kao Corporation | Ester-containing working fluid composition for refrigerating machine |
Cited By (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6998065B1 (en) * | 1989-12-28 | 2006-02-14 | Nippon Mitsubishi Oil Corporation | Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants |
| US6582621B1 (en) * | 1989-12-28 | 2003-06-24 | Nippon Mitsubishi Oil Corporation | Refrigerator oils for use with chlorine-free fluorocarbon refrigerants |
| US7052626B1 (en) * | 1989-12-28 | 2006-05-30 | Nippon Mitsubishi Oil Corporation | Fluid compositions containing refrigeration oils and chlorine-free fluorocarbon refrigerants |
| US6258293B1 (en) * | 1990-11-16 | 2001-07-10 | Hitachi, Ltd. | Refrigeration cycle |
| US6551524B2 (en) | 1992-06-03 | 2003-04-22 | Cognis Corporation | Polyol ester lubricants, especially those compatible with mineral oils, for refrigerating compressors operating at high temperatures |
| US6666985B2 (en) | 1992-06-03 | 2003-12-23 | Cognis Corporation | Polyol ester lubricants for hermetically sealed refrigerating compressors |
| US6551523B1 (en) | 1995-06-07 | 2003-04-22 | Cognis Corporation | Blended polyol ester lubricants for refrigerant heat transfer fluids |
| US6692654B2 (en) * | 1998-09-29 | 2004-02-17 | Nippon Mitsubishi Oil Corporation | Refrigerating machine oil |
| US7018558B2 (en) | 1999-06-09 | 2006-03-28 | Cognis Corporation | Method of improving performance of refrigerant systems |
| US20040092410A1 (en) * | 2002-07-12 | 2004-05-13 | Carr Dale D. | High viscosity synthetic ester lubricant base stock |
| US6774093B2 (en) * | 2002-07-12 | 2004-08-10 | Hatco Corporation | High viscosity synthetic ester lubricant base stock |
| US20050148476A1 (en) * | 2004-01-07 | 2005-07-07 | The Lubrizol Corporation | Automatic transmission fluids with phthalic acid corrosion inhibitor |
| US7429554B2 (en) * | 2004-01-07 | 2008-09-30 | The Lubrizol Corporation | Automatic transmission fluids with phthalic acid corrosion inhibitor |
| US20100038582A1 (en) * | 2007-02-27 | 2010-02-18 | Yuji Shimomura | Refrigerator oil and working fluid composition for refrigerator |
| US9321948B2 (en) | 2007-02-27 | 2016-04-26 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerator |
| US10214671B2 (en) | 2007-02-27 | 2019-02-26 | Jx Nippon Oil & Energy Corporation | Refrigerator oil and working fluid composition for refrigerator |
| US20100038583A1 (en) * | 2007-02-27 | 2010-02-18 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerator |
| US20100051854A1 (en) * | 2007-03-27 | 2010-03-04 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerating machine |
| US8318040B2 (en) | 2007-03-27 | 2012-11-27 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerating machine |
| US20100282999A1 (en) * | 2007-10-29 | 2010-11-11 | Nippon Oil Corporation | Refrigerator oil and working fluid composition for refrigerating machine |
| US8419968B2 (en) * | 2008-11-13 | 2013-04-16 | Chemtura Corporation | Lubricants for refrigeration systems |
| US20100117022A1 (en) * | 2008-11-13 | 2010-05-13 | Chemtura Corporation | Lubricants for refrigeration systems |
| US8858820B2 (en) | 2011-10-07 | 2014-10-14 | American Pacific Corporation | Bromofluorocarbon compositions |
| US20150090921A1 (en) * | 2012-03-23 | 2015-04-02 | Kh Neochem Co., Ltd. | Mixed ester |
| US9523058B2 (en) * | 2012-03-23 | 2016-12-20 | Kh Neochem Co., Ltd. | Mixed ester |
| EP2832813A4 (en) * | 2012-03-30 | 2015-11-11 | Idemitsu Kosan Co | REFRIGERANT COMPOSITION AND METHOD FOR DECREASING DECOMPOSITION OF FLUORINATED HYDROCARBON |
| US9410105B2 (en) | 2012-11-16 | 2016-08-09 | Basf Se | Lubricant compositions comprising epoxide compounds |
| US10000722B2 (en) | 2013-09-12 | 2018-06-19 | Idemitsu Kosan Co., Ltd. | Refrigeration machine oil composition |
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